Human lysophosphatidic acid acyltransferase gamma-2 polypeptide

ABSTRACT

Polypeptides are obtained, for example, via expression of encoding cDNA sequences, that have the activity of the enzyme lysophosphatidic acid acyltransferase (LPAAT), also known as 1-acyl sn-glycerol-3-phosphate acyltransferase.

This is a Divisional Application of application Ser. No. 09/970,989,filed on Oct. 5, 2001, now U.S. Pat. No. 6,670,143, which is aDivisional Application of application Ser. No. 09/215,252, filed on Dec.18, 1998, now U.S. Pat. No. 6,300,487, which is a Continuation-in-Partof application Ser. No. 08/618,651, filed Mar. 19, 1996, now U.S. Pat.No. 6,136,964.

TECHNICAL FIELD OF THE INVENTION

The present invention provides polypeptides having lysophosphatidic acidacyltransferase (LPAAT) activity and polynucleotides encodingpolypeptides having LPAAT activity. The present invention furtherprovides for isolation and production of polypeptides involved inphosphatidic acid metabolism and signaling in mammalian cells, inparticular, the production of purified forms of LPAAT.

BACKGROUND OF THE INVENTION

LPAAT, also referred to as 1-acyl sn-glycerol-3-phosphateacyltransferase (EC 2.3.1.51), is known to catalyze the acylation oflysophosphatidic acid (LPA) to phosphatidic acid (PA) by acylating thesn-2 position of LPA with a fatty acid acyl-chain moiety. LPA and PA,while originally identified as intermediates in lipid biosynthesis(Kent, Anal. Rev. Biochem. 64:315–343, 1995), have more recently beenidentified as phospholipid signaling molecules that affect a wide rangeof biological responses (McPhail et al., Proc. Natl. Acad. Sci. USA92:7931–7935, 1995; Williger et al., J. Biol. Chem. 270:29656–29659,1995; Moolenaar, Curr. Opin. Cell Biol. 7:203–210, 1995).

Cellular activation in monocytic and lymphoid cells is associated withrapid upregulation of synthesis of phospholipids (PL) that includes PA,diacylglycerol (DAG) and glycan phosphatidylinositol (PI). PAs are amolecularly diverse group of phospholipid second messengers coupled tocellular activation and mitogenesis (Singer et al., Exp. Opin. Invest.Drugs 3:631–643, 1994). PA can be generated through hydrolysis ofphosphatidylcholine (PC) (Exton, Biochim. Biophys. Acta 1212:26–42,1994) or glycan PI (Eardley et al., Science 251:78–81, 1991; Merida etal., DNA Cell Biol. 12:473–479, 1993), through phosphorylation of DAG byDAG kinase (Kanoh et al., Trends Biochem. Sci. 15:47–50, 1990) orthrough acylation of LPA at the SN2 position (Bursten et al., Am. J.Physiol. 266:C1093–C1104, 1994).

Compounds that block PA generation and hence diminish lipid biosynthesisand the signal involved in cell activation are therefore of therapeuticinterest in, for example, the areas of inflammation and oncology as wellas obesity treatment. Therefore, compounds that block LPAAT activityhave a similar therapeutic value.

The genes coding for LPAAT have been isolated in bacteria (Coleman, Mol.Gen. Genet. 232:295–303, 1992), in yeast (Nagiec et al., J. Biol. Chem.268:22156–22163, 1993) and in plants (Brown et al., Plant Mol. Biol.26:211–223, 1994; and Hanke et al., Eur J. Biochem. 232:806–810, 1995;Knutzon, et al., Plant Physiol. 109: 999–1006, 1995). Moreover, twohuman isoforms of LPAAT have been reported (West, et al., DNA Cell Biol.6: 691–701, 1997). These isoforms are denominated LPAATα and LPAATβ(West, et al., DNA Cell Biol. 6: 691–701, 1997) and are describedherein. There remains, however, a need for the isolation of additionalmammalian LPAATs, which can be used, for example, to screen forcompounds that inhibit LPAAT activity.

SUMMARY OF THE INVENTION

The present invention provides cDNA sequences, polypeptide sequences,and transformed cells for producing isolated recombinant mammalianLPAAT. The present invention provides four polypeptides corresponding tohuman LPAAT isoforms. These polypeptides are designated hLPAATα,hLPAATβ, hLPAATγ1, hLPAATγ2, and hLPAATδ. The invention further providesfragments of these polypeptides which are biologically active, i.e.,which retain LPAAT activity. LPAAT activity is defined catalyzingacylation of lysophosphatidic acid (LPA) to phosphatidic acid (PA),specifically by acylating the sn-2 position of LPA with a fatty acidacyl-chain moiety.

The present invention further provides nucleic acid sequences encodinghLPAATα, hLPAATβ, hLPAATγ1, hLPAATγ2, and hLPAATδ and polynucleotidescoding for biologically active fragments of hLPAATα, hLPAATβ, hLPAATγ1,hLPAATγ2, and hLPAATδ. The invention further provides “biologicallyactive” polynucleotide fragments, which connotes polynucleotidefragments which encode polypeptides having LPAAT activity. The inventionfurther provides purified LPAATs and antisense oligonucleotides formodulation of expression of the genes coding for LPAAT polypeptides.Assays for screening test compounds for their ability to inhibit LPAATsare also provided.

The present invention includes the following polynucleotides coding forhLPAATα, hLPAATβ, hLPAATγ1, hLPAATγ2, and hLPAATδ. The inventionprovides the DNA sequences of: SEQ ID NO. 1 which encodes for hLPAATα;SEQ ID NO. 7, which encodes hLPAATβ; FIG. 9, which encodes hLPAATγ1 FIG.10, which encodes hLPAATγ2; and FIG. 11, which encodes and hLPAATδ.

The invention further includes the polypeptides for hLPAATα, hLPAATβ,hLPAATγ1, hLPAATγ2, and hLPAATδ, specifically, the amino acid sequencesof: SEQ ID NO. 2, which represents hLPAATα; SEQ ID NO. 8, whichrepresents hLPAATβ; FIG. 9, which represents hLPAATγ1; FIG. 10, whichrepresents hLPAATγ2; and FIG. 11, which represents hLPAATδ.

The invention further comprises biologically active fragments of theamino acid sequences of SEQ ID NO. 2, SEQ ID NO. 8, FIG. 9, FIG. 10, andFIG. 11 or nucleotide fragments of SEQ ID NO. 1, SEQ ID NO. 7, FIG. 9,FIG. 10, and FIG. 11 which encode biologically active LPAAT. Theinvention further includes polynucleotides which due to the degeneracyof the genetic code encode a polypeptide of SEQ ID NO. 2, SEQ. ID NO. 8,FIG. 9, FIG. 10, and FIG. 11. The invention further includespolynucleotides capable of hybridizing to the nucleic acid sequences ofSEQ ID NO. 1, SEQ ID NO. 7, FIG. 9, FIG. 10, and FIG. 11, under highstringency conditions, and which are biologically active.

Also provided by the present invention are vectors containing a DNAsequence encoding a mammalian LPAAT enzyme in operative association withan expression control sequence. Host cells, transformed with suchvectors for use in producing recombinant LPAAT, are also provided withthe present invention. The inventive vectors and transformed cells areemployed in a process for producing recombinant mammalian LPAAT. In thisprocess, a cell line transformed with a DNA sequence encoding LPAAT inoperative association with an expression control sequence, is cultured.The claimed process may employ a number of known cells as host cells forexpression of the LPAAT polypeptide, including, for example, mammaliancells, yeast cells, insect cells and bacterial cells. The presentinvention further provides transformed cells that expresses activemammalian LPAAT.

The present invention further provides methods for identifying compoundsthat increase or decrease LPAAT activity, i.e., acylation of LPA to PA.Because PA concentration is involved in numerous cellular pathways,compounds that increase or decrease acylation of LPA to PA are useful inregulating a number of cellular pathways. Such compounds can be used,for example, to augment trilineage hematopoiesis after cytoreductivetherapy or to inhibit inflammation following hypoxia and reoxygenationinjury (e.g., sepsis, trauma, and ARDS). Moreover, the present inventioncontemplates the use of such compounds in an in vitro or in vivocontext.

The present invention further includes: An isolated polynucleotideencoding a polypeptide having Lysophosphatidic Acid Acyltransferase(LPAAT) activity, comprising a nucleotide sequence selected from thegroup consisting of:

(a) the DNA sequence of FIG. 9, FIG. 10, or FIG. 11 and biologicallyactive fragments thereof; and

(b) a DNA sequence which encodes the polypeptide of FIG. 9, FIG. 10, orFIG. 11 and biologically active fragments thereof.

An isolated polypeptide having LPAAT activity, comprising the amino acidsequence of FIG. 9, FIG. 10, or FIG. 11 and biologically activefragments thereof.

A method for screening one or more compounds to determine whether theone or more compounds increases or decreases LPAAT activity, comprising:

(a) contacting the polypeptide of the present invention with one or moresubstrates for the polypeptide and with the one or more compounds; and

(b) measuring whether the LPAAT activity of the polypeptide is increasedor decreased by the one or more compounds.

A method of expressing the polypeptide of the present invention,comprising:

(a) introducing into a cell a polynucleotide comprising a nucleotidesequence selected from the group consisting of:

-   -   (i) the DNA sequence of FIG. 9, FIG. 10, or FIG. 11 and        biologically active fragments thereof; and    -   (ii) a DNA sequence which encodes the polypeptide of FIG. 9,        FIG. 10, or FIG. 11 and biologically active fragments thereof,    -   wherein the polynucleotide is operably linked to a promoter; and

(b) maintaining or growing said cell under conditions that result in theexpression of the polypeptide.

An isolated polynucleotide encoding a polypeptide havingLysophosphatidic Acid Acyltransferase (LPAAT) activity, comprising a DNAsequence capable of hybridizing under high stringency conditions to thecomplement of the DNA sequences, (a) or (b), described above, and whichencodes a polypeptide having LPAAT activity.

BRIEF DESCRIPTION OF THE DRAWINGS

FIG. 1 shows the DNA sequence (SEQ ID NO: 1) of the cDNA insert ofpZplat.11 encoding hLPAATα (SEQ ID NO: 2).

FIG. 2 shows amino acid sequence alignment of the human LPAATα (SEQ IDNO: 2) coding sequence, the yeast LPAAT (SEQ ID NO: 3) coding sequence,E. coli LPAAT (SEQ ID NO: 4) coding sequence, and the maize LPAAT (SEQID NO: 5) coding sequence. This comparison shows that human LPAATα hasthe greatest extended homology with yeast or E. coli LPAAT than with theplant LPAAT.

FIG. 3 shows the DNA sequence (SEQ ID NO: 6) of the cDNA insertpSP.LPAT3 encoding hLPAATβ. The nucleotide sequence analysis andrestriction mapping of the cDNA clone revealed a 5′ untranslated regionof 39 base pairs and an open reading frame encoding a 278 amino acidpolypeptide that spans positions 40–876. It also shows a 3′ untranslatedregion of 480 base pairs from pSP.LPAT3. The initiation site fortranslation was localized at nucleotide positions 40–42 and fulfilledthe requirement for an adequate initiation site (Kozak, Critical Rev.Biochem. Mol. Biol. 27:385–402, 1992).

FIG. 4 shows the sequence of the hLPAATβ 278 (SEQ ID NOS: 6 & 7) aminoacid open reading frame. The amino acid sequence was used as the querysequence to search for homologous sequences in protein databases. Searchof the database based on Genbank Release 92 from the National Center forBiotechnology Information (NCBI) using the blastp program showed thatthis protein was most homologous to the yeast, bacterial and plantLPAATs.

FIG. 5 shows amino acid sequences alignment of this putative humanLPAATβ (SEQ ID NO: 7) coding sequence, human LPAATα (SEQ ID NO: 2)coding, the yeast LPAAT (SEQ ID NO: 3) coding sequence, the bacterial(E. coli (SEQ ID NO: 4), H. influenzae (SEQ ID NO: 8), and S.typhimurium (SEQ ID NO: 9)) LPAAT coding sequences, and the plant (L.douglassi (SEQ ID NO: 10) and C. nucifera (SEQ ID NO: 11)) LPAAT codingsequences, revealing that the human LPAAT coding sequences have a muchmore extended homology with the yeast or the bacterial LPAAT than withthe plant LPAAT.

FIG. 6 shows a comparison of LPAAT activity in A549 cells transfectedwith pCE9.LPAAT1 DNA, or no DNA using a TLC (thin layer chromatography)assay. These data are described in more detail in examples 3 and 4.

FIGS. 7 and 8 show a comparison of the production of TNF (FIG. 7) andIL-6 (FIG. 8) between A549 cells transfected with pCE9.LPAAT1 andcontrol A549 cells after stimulation with IL-1β and murine TNF. Thesedata show A549 overexpressing LPAAT produces >5 fold more TNF and >10fold more IL-6 relative to untransfected A549 cells, suggesting thatover expression of LPAAT enhances the cytokine signaling response incells.

FIG. 9 shows the DNA (SEQ ID NO: 12) and the translated sequence ofLPAATγ1 (SEQ ID NO: 13).

FIG. 10 shows the DNA (SEQ ID NO: 14) and the translated sequence ofLPAATγ2 (SEQ ID NO: 15).

FIG. 11 shows the DNA (SEQ ID NO: 16) and the translated sequence ofLPAAT (SEQ ID NO: 17).

FIG. 12 shows the LPAAT amino acid sequence alignment for human LPAATγ1(SEQ ID NO: 13), γ2 (SEQ ID NO: 15) and δ (SEQ ID NO: 17).

FIG. 13 compares the LPAAT activity in ECV304 cells stably transfectedwith the expression plasmids for LPAATα (pCE9.LPAAT-α), LPAATβ(pCE9.LPAAT-β) DNA, LPAATγ1 (pC9LPTγ1), LPAATδ (pC2LPTδ), or the controlvector (pCE9).

DETAILED DESCRIPTION OF THE INVENTION

The present invention provides isolated LPAAT polypeptides and isolatedpolynucleotides encoding LPAAT polypeptides. The term “isolated,” inthis context, denotes a polypeptide or polynucleotide essentially freeof other polypeptides or nucleic acid sequences, respectively, or ofother contaminants normally found in nature.

The invention includes biologically active LPAAT and biologically activefragments thereof. As used herein, the term “biologically active” in thecontext of LPAAT activity refers to the ability to catalyze theacylation of lysophosphatidic acid (LPA) to phosphatidic acid (PA) byacylating the sn-2 position of LPA with a fatty acid acyl-chain moiety.

The term “expression product” as used throughout the specificationrefers to materials produced by recombinant DNA techniques.

The present invention contemplates modification of the hLPAATα, hLPAATβ,hLPAATγ1, hLPAATγ2, and hLPAATδ polypeptide sequences. Suchmodifications may be deliberate, as by site-directed mutagenesis, or maybe spontaneous. All of the polypeptides produced by these modificationsare included herein as long as the acyltransferase activity of LPAAT ispresent.

For example, the present invention contemplates the deletion of one ormore amino acids from the polypeptide sequence of the hLPAATα, hLPAATβ,hLPAATγ1, hLPAATγ2, and hLPAATδ to create deletion variants. Thisdeletion can be of one or more amino or carboxy terminal amino acids orone or more internal amino acids. The present invention furthercontemplates one or more amino acid substitutions to the polypeptidesequence of hLPAATα, hLPAATβ, hLPAATγ1, hLPAATγ2, and hLPAAT to createsubstitutional variants. The present invention contemplates that suchsubstitutional variants would contain certain functional alterations,such as stabilizing against proteolytic cleavage. Yet, it is understoodthat such variants retain their acyltransferase activity.

Substitutions preferably are conservative, that is, one amino acid isreplaced with one of similar shape and charge. Conservativesubstitutions are well known in the art and include, for example, thechanges of: alanine to serine; arginine to lysine; asparigine toglutamine or histidine; aspartate to glutamate; cysteine to serine;glutamine to asparigine; glutamate to aspartate; glycine to proline;histidine to asparigine or glutamine; isoleucine to leucine or valine;leucine to valine or isoleucine; lysine to arginine, glutamine, orglutamate; methionine to leucine or isoleucine; phenylalanine totyrosine, leucine or methionine; serine to threonine; threonine toserine; tryptophan to tyrosine; tyrosine to tryptophan or phenylalanine;and valine to isoleucine or leucine.

The present invention further contemplates the insertion of one or moreamino acids to the polypeptide sequences of hLPAATα, hLPAATβ, hLPAATγ1,hLPAATγ2, and hLPAATδ to create an insertional variant. Examples of suchinsertional variants include fusion proteins such as those used to allowrapid purification of the polypeptide and also can include hybridpolypeptides containing sequences from other proteins and polypeptideswhich are homologues of the inventive polypeptide. For example, aninsertional variant could include portions of the amino acid sequence ofthe polypeptide from one species, together with portions of thehomologous polypeptide from another species. Other insertional variantscan include those in which additional amino acids are introduced withinthe coding sequence of the polypeptides. These typically are smallerinsertions than the fusion proteins described above and are introduced,for example, to disrupt a protease cleavage site.

Polypeptides of the present invention can be synthesized by suchcommonly used methods as t-BOC or FMOC protection of alpha-amino groups.Both methods involve step-wise syntheses whereby a single amino acid isadded at each step starting from the C terminus of the peptide (Coliganet al., Current Protocols in Immunology, Wiley Interscience, Unit 9,1991). In addition, polypeptide of the present invention can also besynthesized by solid phase synthesis methods (e.g., Merrifield, J. Am.Chem. Soc. 85:2149, 1962; and Steward and Young, Solid Phase PeptideSynthesis, Freeman, San Francisco pp. 27–62, 1969) using copolyol(styrene-divinylbenzene) containing 0.1–1.0 mM amines/g polymer. Oncompletion of chemical synthesis, the polypeptides can be deprotectedand cleaved from the polymer by treatment with liquid HF 10% anisole forabout 15–60 min at 0° C. After evaporation of the reagents, the peptidesare extracted from the polymer with 1% acetic acid solution, which isthen lyophilized to yield crude material. This can normally be purifiedby such techniques as gel filtration of Sephadex G-15 using 5% aceticacid as a solvent. Lyophilization of appropriate fractions of the columnwill yield a homogeneous polypeptide or polypeptide derivatives, whichare characterized by such standard techniques as amino acid analysis,thin layer chromatography, high performance liquid chromatography,ultraviolet absorption spectroscopsy, molar rotation, solubility andquantitated by solid phase Edman degradation.

The invention also provides polynucleotides which encode the hLPAATpolypeptides of the invention. As used herein, “polynucleotide” refersto a polymer of deoxyribonucleotides or ribonucleotides in the form of aseparate fragment or as a component of a larger construct.

Polynucleotide sequences of the invention include DNA, RNA and cDNAsequences. Preferably, the polynucleotide sequences encoding hLPAAT arethe sequences of: SEQ ID NO. 1 for hLPAATα; SEQ ID NO. 7 for LPAATβ;FIG. 9 for hLPAATγ1; FIG. 10 for hLPAATγ2; and FIG. 11 for hLPAATδ. DNAsequences of the present invention can be obtained by several methods.For example, the DNA can be isolated using hybridization procedureswhich are known in the art. Such hybridization procedures include, forexample, hybridization of probes to genomic or cDNA libraries to detectshared nucleotide sequences, antibody screening of expression librariesto detect shared structural features, such as a common antigenicepitope, and synthesis by the polymerase chain reaction (PCR).

Hybridization procedures are useful for screening of recombinant clonesby using labeled mixed synthetic oligonucleotide probes, wherein eachprobe is potentially the complete complement of a specific DNA sequencein a hybridization sample which includes a heterogeneous mixture ofdenatured double-stranded DNA. For such screening, hybridization ispreferably performed on either single-stranded DNA or denatureddouble-stranded DNA. Hybridization is particularly useful for detectionof cDNA clones derived from sources where an extremely low amount ofmRNA sequences relating to the polypeptide of interest are present.Using stringent hybridization conditions directed to avoid non-specificbinding, it is possible to allow an autoradiographic visualization of aspecific cDNA clone by the hybridization of the target DNA to thatsingle probe in the mixture, which is its complement (Wallace et al.Nucl. Acid Res. 9:879, 1981). Stringent conditions preferably includehigh stringency conditions. See, for example, Maniatis et al, MolecularCloning (A Laboratory Manual), Cold Spring Harbor Laboratory, pages387–389, 1982. One such high stringency hybridization condition is, forexample, 4×SSC at 65° C., followed by washing in 0.1×SSC at 65° C. forthirty minutes. Alternatively, another high stringency hybridizationcondition is in 50% formamide, 4×SSC at 42° C.

The development of specific DNA sequences encoding hLPAAT can also beobtained by isolation of double-stranded DNA sequences from the genomicDNA, chemical manufacture of a DNA sequence to provide the necessarycodons for the polypeptide of interest, and in vitro synthesis of adouble-stranded DNA sequence by reverse transcription of mRNA isolatedfor a eukaryotic donor cell. In the latter case, a double-stranded DNAcomplement of mRNA is eventually formed which is generally referred toas cDNA. Of these three methods for developing specific DNA sequencesfor use in recombinant procedures, the isolation of genomic DNA isolatesis the least common. This is especially true when it is desirable toobtain the microbial expression of mammalian polypeptides due to thepresence of introns.

The synthesis of DNA sequences is frequently a method that is preferredwhen the entire sequence of amino acids residues of the desiredpolypeptide product is known. When the entire sequence of amino acidresidues of the desired polypeptide is not known, direct synthesis ofDNA sequences is not possible and it is desirable to synthesize cDNAsequences. cDNA sequence isolation can be done, for example, byformation of plasmid- or phage-carrying cDNA libraries which are derivedfrom reverse transcription of mRNA. mRNA is abundant in donor cells thathave high levels of genetic expression. In the event of lower levels ofexpression, PCR techniques are preferred. When a significant portion ofthe amino acid sequence is known, production of labeled single or doublestranded DNA or RNA probe sequences duplicating a sequence putativelypresent in the target cDNA may be employed in DNA/DNA hybridizationprocedures, carried out on cloned copies of the cDNA (denatured into asingle-stranded form) (Jay et al., Nucl. Acid Res. 11:2325, 1983).

A cDNA expression library, such as lambda gt11, can be screened forhLPAATα, hLPAATβ, hLPAATγ1, hLPAATγ2, and hLPAATδ polypeptides usingantibodies specific for hLPAATα, hLPAATβ, hLPAATγ1, hLPAATγ2, andhLPAATδ. Such antibodies can be either polyclonally or monoclonallyderived.

The polynucleotides of this invention include sequences that aredegenerate as a result of the genetic code. The genetic code isdescribed as degenerate because more than one nucleotide triplet, calleda codon, can code for a single amino acid. The present inventioncontemplates the degeneracy of the genetic code and includes alldegenerate nucleotide sequences which encode hLPAATα, hLPAATβ, hLPAATγ1,hLPAATγ2, and hLPAATδ.

The present invention also includes polynucleotide sequencescomplementary to the polynucleotides encoding hLPAATα, hLPAATβ,hLPAATγ1, hLPAATγ2, and hLPAATδ. Specifically, the present inventionincludes antisense polynucleotides. An antisense polynucleotide is a DNAor RNA molecule complementary to at least a portion of a specific mRNAmolecule (Weintraub, Sci. Amer. 262:40, 1990). The invention embracesall antisense polynucleotides capable of inhibiting the expression ofhLPAATα, hLPAATβ, hLPAATγ1, hLPAATγ2, or hLPAATδ. In a cell, theantisense polynucleotides hybridize to the corresponding mRNA, forming adouble-stranded molecule. The antisense polynucleotides interfere withthe translation of mRNA since the cell cannot translate mRNA that isdouble-stranded. Antisense oligomers of about 15 nucleotides arepreferred, since they are easily synthesized and are less likely tocause problems than larger molecules when introduced into the target ofhLPAATα, hLPAATβ, hLPAATγ1, hLPAATγ2, or hLPAATδ-producing cell. The useof antisense methods to inhibit translation of genes is known (e.g.,Marcus-Sakura, Anal. Biochem. 172:289, 1988).

The present invention further includes allelic variations, i.e.,naturally-occurring base changes in a species population which may ormay not result in an amino acid change, to the polynucleotide sequencesencoding hLPAATα, hLPAATβ, hLPAATγ1, hLPAATγ2, or hLPAATδ. The inventivepolynucleotide sequences further comprise those sequences whichhybridize under high stringency conditions (see, for example, Maniatiset al, Molecular Cloning (A Laboratory Manual), Cold Spring HarborLaboratory, pages 387–389, 1982) to the coding regions or to thecomplement of the coding regions of hLPAATα, hLPAATβ, hLPAATγ1,hLPAATγ2, or hLPAATδ. One such high stringency hybridization conditionis, for example, 4×SSC at 65° C., followed by washing in 0.1×SSC at 65°C. for thirty minutes. Alternatively, another high stringencyhybridization condition is in 50% formamide, 4×SSC at 42° C.

In addition, ribozyme nucleotide sequences that cleave hLPAATα, hLPAATβ,hLPAATγ1, hLPAATγ2, and hLPAATδ are included in this invention.Ribozymes are RNA molecules possessing an ability to specifically cleaveother single-stranded RNA in a manner analogous to DNA restrictionendonucleases. Through the modification of nucleotide sequences whichtranscribe such RNAs, it is possible to engineer molecules thatrecognize specific nucleotide sequences in an RNA molecule and cleave it(Cech, J. Amer. Med. Assn. 260:3030, 1988).

There are two basic types of ribozymes, tetrahymena-type (Hasselhoff,Nature 334:585, 1988) and “hammerhead-type”. Tetrahymena-type ribozymesrecognize sequences which are four bases in length, while“hammerhead-type” ribozymes recognize base sequences 11–18 bases inlength. The longer the recognition sequence, the greater the likelihoodthat the sequence will occur exclusively in the target mRNA species.Consequently, hammerhead-type ribozymes are preferable totetrahymena-type ribozymes for inactivating a specific mRNA species.

Production of Polypeptides

Polynucleotide sequences encoding hLPAATα, hLPAATβ, hLPAATγ1, hLPAATγ2,and hLPAATδ polypeptides of the invention can be expressed in eitherprokaryotes or eukaryotes. Hosts can include microbial (bacterial),yeast, insect and mammalian organisms. Methods of expressing DNAsequences inserted downstream of prokaryotic or viral regulatorysequences in prokaryotes are known in the art (Makrides, Microbio. Rev.60:512, 1996). Biologically functional viral and plasmid DNA vectorscapable of expression and replication in a eukaryotic host are known inthe art (Cachianes, Biotechniques 15:255, 1993). Such vectors are usedto incorporate DNA sequences of the invention. DNA sequences encodingthe inventive polypeptides can be expressed in vitro by DNA transferinto a suitable host using known methods of transfection.

hLPAATα, hLPAATβ, hLPAATγ1, hLPAATγ2, and hLPAATδ sequences may beinserted into a recombinant expression vector. The term “recombinantexpression vector” refers to a plasmid, virus or other vehicle that hasbeen manipulated by inserting or incorporating genetic sequences. Suchexpression vectors contain a promoter sequence which facilitatesefficient transcription of the inserted genetic sequence of the host.The expression vector typically contains an origin of replication and apromoter, as well as specific genes which allow phenotypic selection ofthe transformed cells. The DNA segment can be present in the vector,operably linked to regulatory elements, for example, a promoter (e.g.,T7, metallothionein I, or polyhedren promoters). Vectors suitable foruse in the present invention include, for example, bacterial expressionvectors, with bacterial promoter and ribosome binding sites, forexpression in bacteria (Gold, Meth. Enzymol. 185:11, 1990), expressionvector with animal promoter and enhancer for expression in mammaliancells (Kaufman, Meth. Enzymol. 185:487, 1990) and baculovirus-derivedvectors for expression in insect cells (Luckow et al., J. Virol.67:4566, 1993).

The vector may include a phenotypically selectable marker to identifyhost cells which contain the expression vector. Examples of markerstypically used in prokaryotic expression vectors include antibioticresistance genes for ampicillin (β-lactamases), tetracycline andchloramphenicol (chloramphenicol acetyltransferase). Examples of suchmarkers typically used in mammalian expression vectors include the genefor adenosine deaminase (ADA), aminoglycoside phosphotransferase (neo,G418), dihydrofolate reductase (DHFR), hygromycin-B-phosphotransferase(HPH), thymidine kinase (TK), and xanthine guaninephosphoriboseyltransferase (XGPRT, gpt).

In another preferred embodiment, the expression system used is onedriven by the baculovirus polyhedrin promoter. The polynucleotideencoding LPAAT can be manipulated by standard techniques in order tofacilitate cloning into the baculovirus vector. See Ausubel et al.,supra. A preferred baculovirus vector is the pBlueBac vector(Invitrogen, Sorrento, Calif.). The vector carrying a polynucleotideencoding LPAAT is transfected into Spodoptera frugiperda (Sf9) cells bystandard protocols, and the cells are cultured and processed to producethe recombinant polypeptide. See Summers et al., A Manual for Methods ofBaculovirus Vectors and Insect Cell Culture Procedures, TexasAgricultural Experimental Station.

The polynucleotides of the present invention can be expressed in anynumber of different recombinant DNA expression systems to generate largeamounts of polypeptide. Included within the present invention are LPAATpolypeptides having native glycosylation sequences, and deglycosylatedor unglycosylated polypeptides prepared by the methods described below.Examples of expression systems known to the skilled practitioner in theart include bacteria such as E. coli, yeast such as Pichia pastoris,baculovirus, and mammalian expression systems such as in Cos or CHOcells.

The polynucleotides of the present invention can be inserted into anexpression vector by standard subcloning techniques. In a preferredembodiment, an E. coli expression vector is used which produces therecombinant protein as a fusion protein, allowing rapid affinitypurification of the protein. Examples of such fusion protein expressionsystems are the glutathione S-transferase system (Pharmacia, Piscataway,N.J.), the maltose binding protein system (NEB, Beverley, Mass.), thethiofusion system (Invitrogen, San Diego, Calif.), the Strep-tag IIsystem (Genosys, Woodlands, Tex.), the FLAG system (IBI, New Haven,Conn.), and the 6xHis (SEQ ID NO: 43) system (Qiagen, Chatsworth,Calif.). Some of these systems produce recombinant polypeptides bearingonly a small number of additional amino acids, which are unlikely toaffect the LPAAT ability of the recombinant polypeptide. For example,both the FLAG system and the 6xHis (SEQ ID NO: 43) system add only shortsequences, both of which are known to be poorly antigenic and which donot adversely affect folding of the polypeptide to its nativeconformation. Other fusion systems produce proteins where it isdesirable to excise the fusion partner from the desired protein. In apreferred embodiment, the fusion partner is linked to the recombinantpolypeptide by a peptide sequence containing a specific recognitionsequence for a protease. Examples of suitable sequences are thoserecognized by the Tobacco Etch Virus protease (Life Technologies,Gaithersburg, Md.) or Factor Xa (New England Biolabs, Beverley, Mass.)or enterokinase (Invitrogen, San Diego, Calif.).

In an embodiment of the present invention, the polynucleotides encodingLPAAT are analyzed to detect putative transmembrane sequences. Suchsequences are typically very hydrophobic and are readily detected by theuse of standard sequence analysis software, such as MacDNASIS (Hitachi,San Bruno, Calif.). The presence of transmembrane sequences is oftendeleterious when a recombinant protein is synthesized in many expressionsystems, especially in E. coli, as it leads to the production ofinsoluble aggregates which are difficult to renature into the nativeconformation of the polypeptide.

Accordingly, deletion of one or more of the transmembrane sequences maybe desirable. Deletion of transmembrane sequences typically does notsignificantly alter the conformation or activity of the remainingpolypeptide structure. However, one can determine whether deletion ofone or more of the transmembrane sequences has effected the biologicalactivity of the LPAAT protein by, for example, assaying the activity ofthe LPAAT protein containing one or more deleted sequences and comparingthis activity to that of unmodified LPAAT. Assaying LPAAT activity canbe accomplished by, for example, contacting the LPAAT protein ofinterest with the substrates LPA and fatty acyl-CoA and measuring thegeneration of PA or CoA, or, alternatively, measuring the formation offree CoA. Such assays for determining LPAAT activity are described inmore detail below in the section describing screening assays.

Moreover, transmembrane sequences, being by definition embedded within amembrane, are inaccessible as antigenic determinants to a host immunesystem. Antibodies to these sequences will not, therefore, provideimmunity to the host and, hence, little is lost in terms of generatingmonoclonal or polyclonal antibodies by omitting such sequences from therecombinant polypeptides of the invention. Deletion oftransmembrane-encoding sequences from the polynucleotide used forexpression can be achieved by standard techniques. See Ausubel et al.,supra, Chapter 8. For example, fortuitously-placed restriction enzymesites can be used to excise the desired gene fragment, or the PCR can beused to amplify only the desired part of the gene.

Transformation of a host cell with recombinant DNA may be carried out byconventional techniques. When the host is prokaryotic, such as E. coli,competent cells which are capable of DNA uptake can be prepared fromcells harvested after exponential growth phases and subsequently treatedby a CaCl₂ method using standard procedures. Alternatively, MgCl₂ orRbCl can be used. Transformation can also be performed after forming aprotoplast of the host cell or by electroporation.

When the host is a eukaryote, methods of transfection of DNA, such ascalcium phosphate co-precipitates, conventional mechanical procedures,(e.g., microinjection), electroporation, liposome-encased plasmids, orvirus vectors may be used. Eukaryotic cells can also be cotransformedwith DNA sequences encoding hLPAATα, hLPAATβ, hLPAATγ1, hLPAATγ2, andhLPAATδ polypeptides of the invention, and a second foreign DNA moleculeencoding a selectable phenotype, such as the herpes simplex thymidinekinase gene. Another method uses a eukaryotic viral vector, such assimian virus 40 (SV40) or bovine papilloma virus to transiently infector transform eukaryotic cells and express the hLPAATα, hLPAATβ,hLPAATγ1, hLPAATγ2, and hLPAATδ polypeptides.

Expression vectors that are suitable for production of LPAATpolypeptides preferably contain (1) prokaryotic DNA elements coding fora bacterial replication origin and an antibiotic resistance marker toprovide for the growth and selection of the expression vector in abacterial host; (2) eukaryotic DNA elements that control initiation oftranscription, such as a promoter; and (3) DNA elements that control theprocessing of transcripts, such as a transcriptiontermination/polyadenylation sequence. LPAAT polypeptides of the presentinvention preferably are expressed in eukaryotic cells, such asmammalian, insect and yeast cells. Mammalian cells are especiallypreferred eukaryotic hosts because mammalian cells provide suitablepost-translational modifications such as glycosylation. Examples ofmammalian host cells include Chinese hamster ovary cells (CHO-K1; ATCCCCL61), rat pituitary cells (GH₁; ATCC CCL82), HeLa S3 cells (ATCCCCL2.2), rat hepatoma cells (H-4-II-E; ATCC CRL1548) SV40-transformedmonkey kidney cells (COS-1; ATCC CRL 1650) and murine embryonic cells(NIH-3T3; ATCC CRL 1658). For a mammalian host, the transcriptional andtranslational regulatory signals may be derived from viral sources, suchas adenovirus, bovine papilloma virus, simian virus, or the like, inwhich the regulatory signals are associated with a particular gene whichhas a high level of expression. Suitable transcriptional andtranslational regulatory sequences also can be obtained from mammaliangenes, such as actin, collagen, myosin, and metallothionein genes.

Transcriptional regulatory sequences include a promoter regionsufficient to direct the initiation of RNA synthesis. Suitableeukaryotic promoters include the promoter of the mouse metallothionein Igene (Hamer et al., J. Molec. Appl. Genet. 1:273,1982); the TK promoterof Herpes virus (McKnight, Cell 31: 355, 1982); the SV40 early promoter(Benoist et al., Nature 290:304, 1981); the Rous sarcoma virus promoter(Gorman et al., Proc. Nat'l. Acad. Sci. USA 79:6777, 1982); and thecytomegalovirus promoter (Foecking et al., Gene 45:101, 1980).Alternatively, a prokaryotic promoter, such as the bacteriophage T3 RNApolymerase promoter, can be used to control fusion gene expression ifthe prokaryotic promoter is regulated by a eukaryotic promoter (Zhou etal., Mol. Cell. Biol. 10:4529, 1990; Kaufman et al., Nucl. Acids Res.19:4485, 1991).

An expression vector can be introduced into host cells using a varietyof techniques including calcium phosphate transfection,liposome-mediated transfection, electroporation, and the like.Preferably, transfected cells are selected and propagated wherein theexpression vector is stably integrated in the host cell genome toproduce stable transformants. Techniques for introducing vectors intoeukaryotic cells and techniques for selecting stable transformants usinga dominant selectable marker are described, for example, by Ausubel andby Murray (ed.), Gene Transfer and Expression Protocols (Humana Press1991). Examples of mammalian host cells include COS, BHK, 293 and CHOcells.

Purification of Recombinant Polypeptides.

The LPAAT polypeptide expressed in any of a number of differentrecombinant DNA expression systems can be obtained in large amounts andtested for biological activity. The recombinant bacterial cells, forexample E. coli, are grown in any of a number of suitable media, forexample LB, and the expression of the recombinant polypeptide induced byadding IPTG to the media or switching incubation to a highertemperature. After culturing the bacteria for a further period ofbetween 2 and 24 hours, the cells are collected by centrifugation andwashed to remove residual media. The bacterial cells are then lysed, forexample, by disruption in a cell homogenizer and centrifuged to separatethe dense inclusion bodies and cell membranes from the soluble cellcomponents. This centrifugation can be performed under conditionswhereby the dense inclusion bodies are selectively enriched byincorporation of sugars such as sucrose into the buffer andcentrifugation at a selective speed. If the recombinant polypeptide isexpressed in the inclusion, these can be washed in any of severalsolutions to remove some of the contaminating host proteins, thensolubilized in solutions containing high concentrations of urea (e.g., 8M) or chaotropic agents such as guanidine hydrochloride in the presenceof reducing agents such as β-mercaptoethanol or DTT (dithiothreitol). Atthis stage it may be advantageous to incubate the polypeptide forseveral hours under conditions suitable for the polypeptide to undergo arefolding process into a conformation which more closely resembles thatof the native polypeptide. Such conditions generally include lowpolypeptide (concentrations less than 500 mg/ml), low levels of reducingagent, concentrations of urea less than 2 M and often the presence ofreagents such as a mixture of reduced and oxidized glutathione whichfacilitate the interchange of disulphide bonds within the proteinmolecule. The refolding process can be monitored, for example, bySDS-PAGE or with antibodies which are specific for the native molecule.Following refolding, the polypeptide can then be purified further andseparated from the refolding mixture by chromatography on any of severalsupports including ion exchange resins, gel permeation resins or on avariety of affinity columns.

Isolation and purification of host cell expressed polypeptide, orfragments thereof may be carried out by conventional means including,but not limited to, preparative chromatography and immunologicalseparations involving monoclonal or polyclonal antibodies.

These polypeptides may be produced in a variety of ways, including viarecombinant DNA techniques, to enable large scale production of pure,biologically active hLPAATα, hLPAATβ, hLPAATγ1, hLPAATγ2, and hLPAATδuseful for screening compounds for, e.g., trilineage hematopoietic andanti-inflammatory therapeutic applications, and developing antibodiesfor therapeutic, diagnostic and research use.

Screening Assays

The hLPAATα, hLPAATβ, hLPAATγ1, hLPAATγ2, and hLPAATδ polypeptides ofthe present invention are also useful in a screening methodology foridentifying compounds or compositions which affect cellular signaling ofan inflammatory response. Such compounds or compositions to be testedcan be selected from a combinatorial chemical library or any othersuitable source (Hogan, Jr., Nat. Biotechnology 15:328, 1997).

This method comprises, for example, contacting hLPAATα, hLPAATβ,hLPAATγ1, hLPAATγ2, and/or hLPAATδ in the presence of compound andsubstrate for LPAAT, namely LPA and fatty acyl-CoA. These hLPAATproteins can either be purified prior to incubation or can be containedin extracts from a cell line or cell lines (for example, Sf9, ECV304,A549) transfected with cDNA encoding these polypeptides (West et al.,DNA Cell Biol. 16;691, 1997). Alternatively, hLPAAT protein can bepurified from transfected cells, and the protein, being a transmembraneprotein, can then be reconstituted in a lipid bilayer to form liposomesfor delivery into cells (Weiner, Immunomethods 4:201, 1994).

The effect of a compound or composition on hLPAATα, hLPAATβ, hLPAATγ1,hLPAATγ2, or hLPAATδ activity can be determined, for example, bymeasuring the generation of PA and CoA. PA can be measured by, forexample, TLC methods described in Examples 3 and 7, found below.Alternatively, LPAAT activity can be assayed by detecting the formationof free CoA in reaction. CoA, which contains a free sulfhydryl-group,can be measured either by, for example, colorimetric or fluorescenicmethods with sulfhydryl-specific reagents, such as,5,5′-dithiobis-(2-nitrobenzoic acid) (DTNB) or ThioGlo (CovalentAssociates, Woburn, Mass.). The observed effect on hLPAATα, hLPAATβ,hLPAATγ1, hLPAATγ2, and hLPAATδ may be either inhibitory or stimulatory.

Peptide Sequencing

Purified polypeptides prepared by the methods described above can besequenced using methods well known in the art, for example using a gasphase peptide sequencer (Applied Biosystems, Foster City, Calif.).Because the proteins of the present invention may be glycosylated, it ispreferred that the carbohydrate groups are removed from the proteinsprior to sequencing. This can be achieved by using glycosidase enzymes.Preferably, glycosidase F (Boehringer-Mannheim, Indianapolis, Ind.) isused. To determine as much of the polypeptide sequence as possible, itis preferred that the polypeptides of the present invention be cleavedinto smaller fragments more suitable for gas-phase sequence analysis.This can be achieved by treatment of the polypeptides with selectivepeptidases, and in a particularly preferred embodiment, withendoproteinase lys-C (Boehringer). The fragments so produced can beseparated by reversed-phase HPLC chromatography.

Antibodies Directed to LPAAT

Antibodies to human LPAAT can be obtained using the product of an LPAATexpression vector or synthetic peptides derived from the LPAAT codingsequence coupled to a carrier (Pasnett et al., J. Biol. Chem. 263:1728,1988) as an antigen. The preparation of polyclonal antibodies iswell-known to those of skill in the art. See, for example, Green et al.,“Production of Polyclonal Antisera,” in Immunochemical Protocols(Manson, ed.), pages 1–5 (Humana Press 1992). Alternatively, an LPAATantibody of the present invention may be derived from a rodentmonoclonal antibody (MAb). Rodent monoclonal antibodies to specificantigens may be obtained by methods known to those skilled in the art.See, for example, Kohler and Milstein, Nature 256:495, 1975, and Coliganet al. (eds.), Current Protocols in Immunology, 1:2.5.1–2.6.7 (JohnWiley & Sons 1991). Briefly, monoclonal antibodies can be obtained byinjecting mice with a composition comprising an antigen, verifying thepresence of antibody production by removing a serum sample, removing thespleen to obtain B-lymphocytes, fusing the B-lymphocytes with myelomacells to produce hybridomas, cloning the hybridomas, selecting positiveclones which produce antibodies to the antigen, culturing the clonesthat produce antibodies to the antigen, and isolating the antibodiesfrom the hybridoma cultures.

MAbs can be isolated and purified from hybridoma cultures by a varietyof well-established techniques. Such isolation techniques includeaffinity chromatography with Protein-A Sepharose, size-exclusionchromatography, and ion-exchange chromatography. See, for example,Coligan at pages 2.7.1–2.7.12 and pages 2.9.1–2.9.3. Also, see Baines etal., “Purification of Immunoglobulin G (IgG),” in Methods in MolecularBiology, 10:79–104 Humana Press, Inc. 1992. An LPAAT antibody of thepresent invention may also be derived from a subhuman primate antibody.General techniques for raising therapeutically useful antibodies inbaboons may be found, for example, in Goldenberg et al., internationalpatent publication No. WO 91/11465 (1991), and in Losman et al., Int. J.Cancer 46:310, 1990.

Alternatively, a therapeutically useful LPAAT antibody may be derivedfrom a “humanized” monoclonal antibody. Humanized monoclonal antibodiesare produced by transferring mouse complementary determining regionsfrom heavy and light variable chains of the mouse immunoglobulin into ahuman variable domain, and then, substituting human residues in theframework regions of the murine counterparts. The use of antibodycomponents derived from humanized monoclonal antibodies obviatespotential problems associated with the immunogenicity of murine constantregions. General techniques for cloning murine immunoglobulin variabledomains are described, for example, by the publication of Orlandi etal., Proc. Nat'l. Acad. Sci. USA 86:3833, 1989. Techniques for producinghumanized MAbs are described, for example, by Jones et al., Nature321:522, 1986, Riechmann et al., Nature 332:323, 1988, Verhoeyen et al.,Science 239:1534, 1988, Carter et al., Proc. Nat'l Acad. Sci. USA89:4285, 1992, Sandhu, Crit. Rev. Biotech. 12: 437, 1992, and Singer etal., J. Immun. 150:2844, 1993, each of which is hereby incorporated byreference.

As an alternative, an LPAAT antibody of the present invention may bederived from human antibody fragments isolated from a combinatorialimmunoglobulin library. See, for example, Barbas et al., METHODS: ACompanion to Methods in Enzymology 2:119 1991, and Winter et al., Ann.Rev. Immunol. 12:433, 1994, which are incorporated by reference. Cloningand expression vectors that are useful for producing a humanimmunoglobulin phage library can be obtained, for example, fromSTRATAGENE Cloning Systems (La Jolla, Calif.). In addition, an LPAATantibody of the present invention may be derived from a human monoclonalantibody. Such antibodies are obtained from transgenic mice that havebeen “engineered” to produce specific human antibodies in response toantigenic challenge. In this technique, elements of the human heavy andlight chain locus are introduced into strains of mice derived fromembryonic stem cell lines that contain targeted disruptions of theendogenous heavy chain and light chain loci. The transgenic mice cansynthesize human antibodies specific for human antigens, and the micecan be used to produce human antibody-secreting hybridomas. Methods forobtaining human antibodies from transgenic mice are described by Greenet al., Nature Genet. 7:13, 1994; Lonberg et al., Nature 368:856, 1994,and Taylor et al., Int. Immun. 6:579, 1994.

hLPAATα and hLPAATβ

hLPAATα

Search of the Genbank database of expressed sequence tag (dbest) usingeither the yeast or plant LPAAT protein sequences as probe came up withseveral short stretches of cDNA sequences with homology to the yeast orplant LPAAT protein sequence. These cDNA sequences of interest werederived from single-run partial sequencing of random human cDNA clonesprojects carried out by either the WashU-Merck EST or theGenexpress-Genethon program. An example of the amino acids sequencehomology between the yeast LPAAT and a human cDNA clone (dbest#102250)is shown below by comparing SEQ ID NO. 18 (top amino acid sequence) withSEQ ID NO 19 (bottom amino acid sequence):

PFKKGAFHLAQQGKIPIVPVVVSNTSTLVSPKYGVFNRGCMIVRILKPISTE*   ****** *  **** * *       *  *  *   ** * * **PSNCGAFHLAVQAQVPIVPIVMSSYQDFYCKKERRFTSGQCQVRVLPPVPTE

The top line refers to the yeast LPAAT sequence from amino acids 169 to220 and the bottom line refers to the homologous region from the dbestclone#102250. Identical amino acids between these two sequences areshown in block letters with asterisks in between.

Accordingly, a synthetic oligonucleotide (o.BLPAT.2R),5′-TGCAAGATGGAAGGCGCC-3′ (SEQ ID NO. 20), was made based on thecomplement sequence of the conserved amino acids region, GAFHLA (SEQ IDNO. 21), of clone#102250. o.BPLAT.2R was radiolabeled at its 5′-endusing γ-³²P-ATP and T4 polynucleotide kinase as a probe in screening aλzap human brain cDNA library (Stratagene).

Screening of the cDNA library was accomplished by filter hybridizationusing standard methods (Current Protocols in Molecular Biology, JohnWiley & Sons, Inc., 1995). Duplicate filters containing DNA derived fromλ phage plagues were prehybridized at 60° C. for 2 hr in 6×SSC (1×SSC is0.15 M NaCl, 0.015 M sodium citrate, pH 7.0), 5×Denhardt's solution(1×Denhardt's solution is 0.02% Ficoll, 0.02% bovine serum albumin, and0.02% polyvinyl-pyrrolidone), 0.1% sodium dodecyl sulfate (SDS), 50mg/ml sonicated and denatured salmon sperm DNA. Hybridization wascarried out in the same buffer as used for prehybridzation. Afterhybridization, the filters were washed in 6×SSC at 42° C., andautoradiographed.

Of the approximately 1×10⁶ clones from the human brain cDNA library thatwere screened, twelve clones were identified that hybridized with theprobe in duplicate filters. Eleven out twelve clones were enriched andrecovered after a secondary screen. Ten enriched phage samples were thenconverted to plasmid transformed cells by co-infecting E. coli XL1-Bluewith the helper phage R408 using Stratagene's recommended procedure.Colony filter hybridization was performed and identified those coloniesthat “lit up” with the probe. Seven out of the ten pools of coloniescontained positive clones. Two out of these seven clones, pZlpat.10 andpZlpat.11, contained inserts >2 kb. Restriction mapping using acombination of Sst I, Pst I and BamHI digests showed these two clonescontained many common fragments with respect to each other.

Nucleotide sequencing of the cDNA inserts in pZlpat.10 and pZlpat.11 wasperformed. FIG. 1 shows the DNA sequence of the cDNA insert ofpZplat.11. The nucleotide sequence analysis and restriction mapping ofthe cDNA clone revealed a 5′-untranslated region of >300 bp, an openreading frame capable of encoding a 283 amino acid polypeptide, and a3′-untranslated region of >800 bp. The initiation site for translationwas localized at nucleotide positions 319–321 and fulfilled therequirement for an adequate initiation site according to Kozak (Kozak,Critical Rev. Biochem. Mol. Biol. 27:385–402, 1992). There was anotherupstream ATG at positions 131–133 with an in-phase stop codon atpositions 176–178. Except with a shorter 5′-untranslated region, thecDNA insert of pZplat.10 has the same DNA sequence as that of pZplat.11.

The sequence of the 283 amino acid open reading frame in pZplat.11 wasused as the query sequence to search for homologous sequences in proteindatabases. Search of the database based on Genbank Release 90 from theNational Center for Biotechnology Information (NCBI) using the blastpprogram showed that the protein encoded by pZplat.11 was most homologousto the yeast and bacterial LPAATs. FIG. 2 shows amino acid sequencesalignment of the putative human LPAATα coding sequence, the yeast LPAATcoding sequence, the E. coli LPAAT coding sequence, and the maize LPAATcoding sequence, revealing that human LPAATα has a much more extendedhomology with the yeast or the E. coli LPAAT than with the plant LPAAT.

hLPAATβ

Search of the Genbank database (Boguski, et al., Science 265:1993–1994,1994) of expressed sequence tag (dbEST) using either the yeast or plantLPAAT protein sequences as probe came up with several short stretches ofcDNA sequences with homology to the yeast or plant LPAAT proteinsequence. These cDNA sequences of interest were derived from single-runpartial sequencing of random human cDNA clones projects carried outmainly by I.M.A.G.E. Consortium [LLNL] cDNA clones program. An exampleof the amino acids sequence homology between the yeast LPAAT and a humancDNA clone (dbEST#363498) is shown below:

180       190       200       210       220       230QQGKIPIVPVVVSNTSTLVSPKYGVFNRGCMIVRILKPISTENLTKDKIGEFAEKVRDQM  ....:::::: :. :.. ..:   :..: ..:..:..:.:..:: ... ..VRENVPIVPVVYSSFSSFYNTKKKFFTSGTVTVQVLEAIPTSGLTAADVPALRGTPATGP         70        80        90       100       110 120

The top line refers to the yeast LPAAT sequence from amino acids 171 to230 (SEQ ID NO. 22) and the bottom line refers to the homologous regionfrom the dbest clone#363498 using the +1 reading frame (SEQ ID NO. 23).Identical and conserved amino acids between these two sequences areshown with double dots and single dot, respectively, in between. Inorder to find out if such cDNA clones with limited homology to yeastLPAAT sequence indeed encode human LPAATβ sequence, it was necessary toisolate the full-length cDNA clone, insert it into an expression vector,and to test if cells transformed or transfected with the cDNA expressionvector produced more LPAAT activity.

Accordingly, two synthetic oligonucleotides, 5′-CCTCAAAGTGTGGATCTATC-3′(o.LPAT3.F) (SEQ ID NO. 24) and 5′-GGAAGAGTACACCACGGGGAC-3′ (o.LPAT3.R),(SEQ ID NO. 25) were ordered (Life Technologies, Gaithersburg, Md.)based on, respectively, the coding and the complement sequence ofclone#363498. o.LPAT3.R was used in combination with a forward vectorprimer (o.sport.1), 5′-GACTCTAGCCTAGGCTTTTG C-3′(SEQ ID NO. 26) foramplification of the 5′-region, while o.LPAT3.F was used in combinationwith a reverse vector primer (o.sport.1R), 5′-CTAGCTTATAATACGACTCAC-3′(SEQ ID NO. 27), for amplification of the 3′-region of potential LPAATβsequences from a pCMV.SPORT human leukocyte cDNA library (LifeTechnologies, Gaithersburg, Md.). A 700 bp PCR fragment derived fromo.sport.1 and o.LPAT3.R amplification was cut with EcoR I beforeinserting in between the Sma I and EcoR I of pBluescript(II)SK(−)(Stratagene, LaJolla, Calif.) to generate pLPAT3.5′. A 900 bp PCRfragment derived from o.sport.1R and o.LPAT3.F amplification was cutwith Xba I before inserting in between the Sma I and Xba I ofpBluescript(II)SK(−) (Stratagene, Lajolla, Calif.) to generatepLPAT3.3′. Nucleotide sequencing analysis of the cDNA inserts from thesetwo plasmids showed they contained overlapping sequences with eachother, sequences that matched with the dbEST#363498 as well as extensivehomology with the yeast LPAAT amino acids sequence (Nagiec et al., J.Biol. Chem. 268:22156–22163, 1993). To assemble the two halves of thecDNA into a full-length clone, the 560 bp Nco I-Nar I fragment frompLPAT3.5′ and the 780 bp Nar I-Xba I fragment from pLPAT3.3′ wereinserted into the Nco I/Xba I vector prepared from pSP-luc+ (Promega,Madison, Wis.) via a three-part ligation to generate pSP.LPAT3.

FIG. 3 shows the DNA sequence ID of the cDNA insert of pSP.LPAT3. Thenucleotide sequence analysis and restriction mapping of the cDNA clonerevealed a 5′-untranslated region of 39 bp, an open reading framecapable of encoding a 278 amino acids polypeptide that spans nucleotidepositions 40 to 876 and a 3′-untranslated region of 480 bp (FIG. 3). Theinitiation site for translation was localized at nucleotide positions40–42 and fulfilled the requirement for an adequate initiation siteaccording to Kozak (Kozak, Critical Rev. Biochem. Mol. Biol. 27:385–402,1992).

The sequence of the 278 amino acid open reading frame (FIG. 4) was usedas the query sequence to search for homologous sequences in proteindatabases. Search of the database based on Genbank Release 92 from theNational Center for Biotechnology Information (NCBI) using the blastpprogram showed that this protein was most homologous to the yeast,bacterial and plant LPAATs. FIG. 5 shows amino acid sequences alignmentof this putative human LPAATβ coding sequence, human LPAATα coding, theyeast LPAAT coding sequence, the bacterial (E. coli, H. influenzae, andS. typhimurium) LPAAT coding sequences, and the plant (L. douglassi andC. nucifera) LPAAT coding sequences, revealing that the human LPAATcoding sequences have a much more extended homology with the yeast orthe bacterial LPAAT than with the plant LPAAT.

hLPAATγ1, hLPAATγ2, or hLPAATδ

Described below is the isolation of human LPAAT isoforms hLPAATγ1,hLPAATγ2, or hLPAATδ, which are distinct from hLPAATα and hLPAATβ.

Search of the Genbank database (Boguski, et al., Science 265:1993–1994,1994) of expressed sequence tag (dbEST) using the maize form-I LPAATprotein (Brown, et al., Plant Mol. Biol. 26: 211–223, 1994) sequences asprobes resulted in the identification of several short stretches ofhuman cDNA sequences with homology to the maize LPAAT protein sequence.These cDNA sequences of interest were derived from single-run partialsequencing of random human cDNA clones projects carried out mainly byI.M.A.G.E. Consortium [LLNL] cDNA clones program. An example of theamino acids sequence homology between the maize LPAAT and a human cDNAclone (GenBank#T55627) is shown below:

150 GLQRLKDFPRPFWLALFVEGTRF 172 (SEQ ID NO: 28) ::.::.:.:  .:. :. :::::GLRRLSDYPEYMWFLLYCEGTRF (SEQ ID NO: 29)

The top line refers to the maize LPAAT sequence from amino acids 150 to172 and the bottom line refers to the homologous region from the dbESTclone with GenBank#T55627. Identical and conserved amino acids betweenthese two sequences are shown as double dots and single dots,respectively, in the row in between. In order to determine if thesehuman cDNA clones with homology to maize LPAAT but distinct from humanLPAATα or LPAATβ indeed encoded human LPAAT, it was undertaken toisolate the full-length cDNA clone, insert it into an expression vector,and to test if cells transformed or transfected with the cDNA expressionvector produced more LPAAT activity.

Accordingly, a synthetic oligonucleotides,5′-GACTACCCCGAGTACATGTGGTTTCTC-3′ (SEQ ID NO: 30) (oLPTg_(—)1F) wasordered (Life Technologies, Gaithersburg, MD) based on the coding regioncorresponding to amino acids DYPEYMWFL (SEQ ID NO: 31) of cloneGenBank#T55627. oLPTg_(—)1F was used in combination with a reversevector primer (o.sport.1R), 5′-CTAGCTTATAATACGACTCAC-3′(SEO ID NO: 32),for amplification of the 3′-region of potential LPAAT sequences from apCMV.SPORT human leukocyte cDNA library (Life Technologies,Gaithersburg, Md.). A 1,000 bp PCR fragment derived from o.sport.1R andoLPTg_(—)1F amplification was cut with Xho I before inserting in betweenthe Sma I and Xho I of pBluescript(II)SK(−) (Stratagene, LaJolla,Calif.) to generate the plasmid pLPTγ_(—)3′. Nucleotide sequencing(performed by the Seattle Biomedical Research Institute sequencingservice) analysis of the cDNA inserts from plasmid pLPTg_(—)3′ showed itcontained sequences that matched with the clone GenBank#T55627 as wellas extensive homology with the C-terminal end of the maize LPAAT aminoacids sequence (Brown, et al., Plant Mol. Biol. 26: 211–223, 1994). Toisolate the 5′-portion of this putative LPAAT clone, a syntheticoligonucleotide, 5′-CACATGTCCGCCTCGTACTTCTTC-3′ (SEQ ID NO: 44)(oLPTg_(—)1R), complementary to a region just downstream of the Bam HIsite of the cDNA within generate the plasmid pLPTg_(—)3′ was used incombination with a forward vector primer (o.sport.1),5′-GACTCTAGCCTAGGCTTTTGC-3′ (SEQ ID NO: 45) for amplification of the5′-region from a pCMV.SPORT human leukocyte cDNA library (LifeTechnologies, Gaithersburg, Md.). The PCR fragments generated were cutwith Acc65 I and BamH I before inserting in between the Acc65 I and BamHI of pBluescript(II)SK(−) (Stratagene, LaJolla, Calif.). DNA sequenceanalysis of two cDNA clones containing, respectively, a 980 bp and a 770bp Acc65 I-BamH I inserts showed they contained sequences thatoverlapped with the cDNA insert of pLPTγ_(—)3′ as well as extensivehomology with the N-terminal end of the maize LPAAT amino acidssequence. The DNA sequence of these two cDNA clones diverged at the5′-regions, suggesting the presence of two alternatively splicedvariants with one variant (pLPγ1_(—)5′) containing an additional 62amino acids at the N-terminus relative to the other one (pLPγ2_(—)5′).To assemble the two halves of each cDNA into full-length clones, the 980bp Acc65I-BamH I fragment from pLPγ1_(—)5′ or the 770 bp Acc65I-BamH Ifragment from pLPγ2_(—)5′ were inserted into the Acc65I/Xho I vectorprepared from pBluescript(II)SK(−) (Stratagene, LaJolla, Calif.) alongwith the 870 bp Bam HI-Xho I fragment from pLPTγ_(—)3′ via a three-partligation to generate pSK_Lpγ1 and pSK_Lpγ2, respectively.

FIG. 9 shows the DNA and the translated sequence (LPAAT-γ1) of the cDNAinsert of pSK_LPγ1. The nucleotide sequence analysis and restrictionmapping of the cDNA clone revealed a 5′-untranslated region of 183 bpwith two ATGs and an in-phase stop codon, an open reading frame capableof encoding a 376 amino acids polypeptide that spans nucleotidepositions 184 to 1314 and a 3′-untranslated region of 345 bp. Theinitiation site for translation was localized at nucleotide positions184–186 and fulfilled the requirement for an adequate initiation site(Kozak, Critical Rev. Biochem. Mol. Biol. 27:385–402, 1992).

FIG. 10 shows the DNA and the translated sequence (hLPAATγ2) of the cDNAinsert of pSK_LPγ2. The nucleotide sequence analysis and restrictionmapping of the cDNA clone revealed a 5′-untranslated region of 232 bpwith two upstream ATGs with in-phase stop codons, an open reading framecapable of encoding a 314 amino acids polypeptide that spans nucleotidepositions 133 to 1177 and a 3′-untranslated region of 346 bp. Theinitiation site for translation was localized at nucleotide positions233–235 and fulfilled the requirement for an adequate initiation site(Kozak, Critical Rev. Biochem. Mol. Biol. 27:385–402, 1992).

The sequence of the 376 amino acid open reading frame of hLPAATγ1 (FIG.9) was used as the query sequence to search for homologous sequences inprotein databases. Search of the Genbank database from the NationalCenter for Biotechnology Information (NCBI) using the tblastn programshowed that this protein was distinct but homologous to a human ESTsequence with GenBank #H18562. Shown below is the amino acid sequencesalignment of LPAAT-γ1 with this putative human LPAAT coding sequence(LPAAT-δ): (SEQ ID NOS 33 & 34)

LPAAT-γ1 MGLLAFLKTQFVLHLLVGFVFVVSGLVINFVQLCTLALWPVSKQLY  46 : :   ::.::. ::.  .::. :::.:: .:: :: :::. :::. LPAAT-δMDLAGLLKSQFLCHLVFCYVFIASGLIINTIQLFTLLLWPINKQLF 340

The top line refers to the human LPAAT-γ1 sequence from amino acids 1 to46 and the bottom line refers to the homologous region from the dbESTclone with GenBank #H18562. Identical and conserved amino acids betweenthese two sequences are shown as double dots and single dots,respectively, in the row in between. The cDNA for this putative LPAAT-δclone (Genome Systems Inc., St. Louis, Mo.) was isolated for furtheranalysis.

FIG. 11 shows the DNA and the translated sequence (LPAAT-δ) of this cDNAinsert. Nucleotide sequence analysis and restriction mapping revealed a5′-untranslated region of 157 bp with an upstream ATG and stop codons inall three reading frames, an open reading frame capable of encoding a378 amino acids polypeptide that spans nucleotide positions 158 to 1294and a 3′-untranslated region of 480 bp. The initiation site fortranslation was localized at nucleotide positions 158–160 and fulfilledthe requirement for an adequate initiation site (Kozak, Critical Rev.Biochem. Mol. Biol. 27:385–402, 1992).

FIG. 12 shows the LPAAT amino acid sequence alignment from the humanisoforms γ1, γ2, and δ. Amino acids identical in at least two sequencesare highlighted. LPAAT-γ1 and LPAAT-δ have an overall amino acid matchof 54% with respect to each other.

EXAMPLE 1

This example illustrates an experiment to determine if the human LPAATαclone encodes a protein with LPAAT activity, an E. coli vectorexpressing the human LPAATα as a fusion protein with β-galactosidase wastransformed into a LPAAT minus strain of E. coli to see if it wouldcomplement the defect in E. coli. Specifically, the 840 bp Bgl II-Nco Ifragment, which spans the coding region of human LPAATα from amino acid68 to beyond the stop codon, derived from pZplat.11 was inserted into aBgl II/Nco I digested cloning vector pLitmus28 (Evans et al.,BioTechniques 19:130–135, 1995) to generate the plasmid p28BgN. Thisplasmid is expected to express the human LPAATα as a fusion proteincontaining the first 16 amino acids of β-galactosidase and the last 216residues of the human LPAATα coding sequence using the lac promoter inpLitmus28. This plasmid was transformed into the E. coli strain JC201(obtained from Dr. Jack Coleman, Louisiana State University). JC201(Coleman, Mol. Gen. Genet. 232:295–303, 1992; Nagiec et al., J. Biol.Chem. 268:22156–22163, 1993; and Brown et al., Plant Mol. Biol.26:211–223, 1994) is deficient in LPAAT activity due to mutation in theplsC locus. This mutation leads to a temperature-sensitive phenotypethat causes JC201 to grow slowly at 37° C., almost not at all at 42° C.,and not at all at 44° C. JC201 transformed with p28BgN was able to grownormally at 44° C. when compared to the wild type strain JC200 (plsC⁺),while JC201 transformed with pLitmus28 vector was not able to supportgrowth at 44° C. These data suggest that the putative human LPAATα cDNAisolated here does possess LPAAT activity, as the last 216 amino acidsof this cDNA is sufficient to complement the defective LPAAT gene (plsC)in JC201.

EXAMPLE 2

To see if the putative human LPAATβ clone encodes a protein with LPAATactivity, an E. coli vector expressing this human LPAATβ as a directproduct was transformed into a LPAAT minus strain of E. coli to see ifit would complement the defect in E. coli. Specifically, the 1350 bp NcoI-Xba I fragment from pSP.LPAT3, which spans the entire coding regionfrom amino acid 1 to beyond the stop codon, was inserted into a NcoI/Xba I digested cloning vector pKK388–1 (Clontech, Palo Alto, Calif.)to generate the plasmid pTrc.LPAT3. This plasmid was transformed intothe E. coli strain JC201 (obtained from Dr. Jack Coleman, LouisianaState University). JC201 (Coleman, Mol. Gen. Genet. 232:295–303, 1992)is deficient in LPAAT activity due to mutation in the plsC locus. Thismutation leads to a temperature-sensitive phenotype that causes JC201 togrow slowly at 37° C., almost not at all at 42° C., and not at all at44° C. JC201 transformed with pTrc.LPAT3 was able to grow normally at44° C. when compared to the wild type strain JC200 (plsC⁺), while JC201transformed with pKK388-1 vector was not able to support growth at 44°C. These data suggest that the putative human LPAATβ cDNA isolated heredoes possess LPAAT activity, as the putative protein product of thiscDNA is able to complement the defective LPAAT gene (plsC) in JC201.

EXAMPLE 3

This example illustrates a group of experiments to see if overexpressionof this human LPAATα would have any effect on mammalian cells. Theentire cDNA insert (˜2,300 bp) from pZplat.11 was cleaved with Asp718 Iand Xho I for insertion into the mammalian expression vector pCE9 togenerate pCE9.LPAAT1. pCE9 was derived from pCE2 with two modifications.The 550 bp BstY I fragment within the elongation factor-1a (EF-1a)intron of pCE2 was deleted. The multiple cloning region of pCE2 betweenthe Asp718 I and BamH I site was replaced with the multiple cloningregion spanning the Asp718 I and Bgl II sites from pLitmus28. Theplasmid pCE2 was derived from pREP7b (Leung, et al., Proc. Natl. Acad.Sci. USA, 92: 4813–4817, 1995) with the RSV promoter region replaced bythe CMV enhancer and the elongation factor-1a (EF-1a) promoter andintron. The CMV enhancer came from a 380 bp Xba I-Sph I fragmentproduced by PCR from pCEP4 (Invitrogen, San Diego, Calif.) using theprimers 5′-GGCTCTAGATATTAATAGTAATCAATTAC-3′ (SEQ ID NO: 35) and5′-CCTCACGCATGCACCATGGTAATAGC-3′ (SEQ ID NO: 36). The EF-1a promoter andintron (Uetsuki, et al., J. Biol. Chem., 264: 5791–5798, 1989) came froma 1200 bp Sph I-Asp718 I fragment produced by PCR from human genomic DNAusing the primers 5′-GGTGCATGCGTGAGGCTCCGGTGC-3′ (SEQ ID NO: 37) and5′-GTAGTTTTCACGGTACCTGAAATGGAAG-3′ (SEQ ID NO: 38). These 2 fragmentswere ligated into a Xba I/Asp718 I digested vector derived from pREP7bto generate pCE2.

pCE9.LPAAT1 DNA was transfected into several mammalian cell lines,including A549 cells, ECV304 cells (American Type Culture Collection,Rockville, Md.), two human cell line that would produce IL-6 and TNFupon stimulation with IL-1b and murine TNF and 293-EBNA cells(Invitrogen, San Diego, Calif.). pCE9.LPAAT1 was digested with BspH Ibefore electroporating into these cell lines with a Cell-Porator™ (LifeTechnologies, Gaithersburg, Md.) using conditions described previously(Cachianes, et al., Biotechniques 15:255–259, 1993). After adherence ofthe transfected cells 24 hours later, the cells were grown in thepresence of 200 μg/ml Hygromycin B (Hyg) (Calbiochem, La Jolla, Calif.)to select for cells that had incorporated both plasmids. Hyg-resistantclones that expressed LPAAT mRNA at a level more than 20 fold higherrelative to untransfected cells based on Northern Blot analysis(Kroczek, et al., Anal. Biochem. 184: 90–95, 1990) were selected forfurther study.

FIG. 6 compares the LPAAT activity in A549 cells and in A549 cellstransfected with pCE9.LPAAT1 DNA using aTLC assay. This screening assayfor LPAAT activity in cell extracts was based on a fluorecent assayusing fluorescent lipid substrates (Ella, et al., Anal. Biochem. 218:136–142, 1994). Instead of using the PC-substrate, BPC (MolecularProbes, Eugene, Oreg.), a synthetic PC that contains an ether linkage atthe SN1 position with a fluorescent Bodipy moiety incorporated into theend of the alkyl-chain at the SN1 position, BPC was converted toBodipy-PA using cabbage phospholipase D (Sigma, St. Louis, Mo.).Bodipy-PA was then converted to Bodipy-LPA using snake venomphospholipase A2. The Bodipy-LPA obtained was purified by preparativeTLC for use in the LPAAT assay. The assay was carried out in total cellextracts resuspended in lysis buffer (Ella, et al., Anal. Biochem. 218:136–142, 1994) supplemented with 0.5 mM ATP, 0.3 mM MgCl₂, 100 μMoleoyl-CoA and 10 μM Bodipy LPA. The samples were incubated for 30 minbefore loading onto TLC plates.

Lane 1 refers to Bodipy LPA incubated with buffer only without any cellextract added. Lane 9 refers to BPC treated with cabbage phospholipase Dfor generating a Bodipy-PA marker. Lanes 2 and 4 refer to Bodipy LPAincubated with control A549 cell extracts with or without lipid A,respectively. Lanes 3 and 5 refer to Bodipy LPA incubated with A549 cellextracts transfected with pCE9.LPAAT1 DNA with or without lipid A,respectively. FIG. 3 shows A549 cells transfected with the LPAAT cDNA(lanes 3 and 5) contain much more LPAAT activity than those of controlcells (lanes 2 and 4) as evidenced by the increased conversion ofBodipy-LPA to Bodipy-PA. Addition of lipid A to the cell extracts haslittle effect on LPAAT activity (lanes 2 vs 4 and 3 vs 5). A549 cellextract also contains a phosphohydrolase activity that convertsBodipy-LPA to Bodipy-monoalkylglycerol (lanes 2 to 5). Interestingly,A549 cells overexpressing LPAAT (lanes 3 and 5) have less of thisactivity compared to control cells (lanes 2 and 4), suggesting thisphosphohydrolase prefers LPA to PA as substrate. There is also anincrease of DAG in transfected cells (lanes 3 and 5) compared to controlcells (lanes 2 and 4) possibly due to partial conversion of the PAformed to DAG from this endogenous phosphohydrolase.

EXAMPLE 4

To see if the expressed LPAAT cDNA clone described here would also useother glycerol-lipids that contain a free-hydroxyl group at the SN2position, the cell extracts were incubated with the substratesNBD-lysoPC (lanes 6 and 7) and NBD-monoacylglycerol (MAG) (lanes 10 and11) to see if there is increased conversion to lysoPC and DAG,respectively. Lane 8 and 12 refer, respectively, to NBD-lysoPC andNBD-MAG incubated with buffer only without any cell extract added. TLCanalysis shows little difference in the lipid profile between thetransfected and control cells (lanes 7 vs 6, lanes 11vs 10), suggestingthe cloned LPAAT enzyme uses LPA as the preferred substrate. It islikely that the acyltransferases for lysoPC (Fyrst, et al., Biochem. J.306:793–799, 1995) and for MAG (Bhat, et al., Biochemistry 34:11237–11244, 1995) represent different enzymes from the LPAAT describedhere.

EXAMPLE 5

pCE9.LPAAT1 DNA was transfected into A549 cells (American Type CultureCollection, Rockville, Md.), a human cell line that would produce IL-6and TNF upon stimulation with IL-1β and murine TNF. pCE9.LPAAT1 wasdigested with BspH I before electroporating into A549 cells with aCell-Porator™ (Life Technologies, Gaithersburg, Md.) using conditionsdescribed previously (Cachianes, et al., Biotechniques 15:255–259,1993). After adherence of the transfected cells 24 hours later, thecells were grown in the presence of 200 μg/ml Hygromycin B (Hyg)(Calbiochem, La Jolla, Calif.) to select for cells that had incorporatedboth plasmids. A Hyg-resistant clone that expressed LPAAT mRNA at alevel more than 20 fold higher relative to untransfected A549 cellsbased on Northern Blot analysis (Kroczek et al., Anal. Biochem.184:90–95, 1990) was selected for further study.

A comparison of the production of TNF (FIG. 7) and IL-6 (FIG. 8) betweenA549 cells transfected with pCE9.LPAAT1 and control A549 cells afterstimulation with IL-1β and murine TNF shows A549 overexpressing LPAATproduces >5 fold more TNF and >10 fold more IL-6 relative tountransfected A549 cells, suggesting that overexpression of LPAAT wouldenhance the cytokine signaling response in cells. Development ofcompounds that would modulate LPAAT activity should therefore be oftherapeutic interest in the field of inflammation.

EXAMPLE 6

Construction of pC9LPTγ1 and pC2LPTδ: The primers5′-ggcccggtaccATGGGCCTGCTGGCCTTCC-3′ (SEQ ID NO: 39) (oLPγ1_(—)1F) and5′-taactcCTCGAGTTATTCCTTTTTCTTAAACTC-3′ (SEQ ID NO: 40) (oLPγ1_(—)1R)were used to amplify the 1100 bp Acc65I-XhoI fragment by PCR from thetemplate pSK_LPg1. The fragment generated was then inserted into aAcc65I/Xho I digested pCE9 (West, et al., DNA Cell Biol. 6: 691–701,1997) expression vector to make pC9LPTγ1. Similarly, the primers5′-atggtggtaccaccATGGACCTCGCGGGACTGCTG-3′ (SEQ ID NO: 41) (oLPTδ_(—)1F)and 5′-GGAgGATATctAGAgGCCACCAGTTC-3′ (SEQ ID NO: 42) (oLPTδ_(—)1R) wereused to amplify the 1100 bp Acc65 I-Xba I fragment by PCR from thetemplate #H18562. The fragment generated was then inserted into aAcc65I/Nhe I digested pCE2 (West, et al., DNA Cell Biol. 6: 691–701,1997) expression vector to make pC2LPTδ.

EXAMPLE 7

Expression of hLPAATγ1 and hLPAATδ in mammalian cells. Plasmids pC9LPTγ1or pC2LPTδ were stably transfected into endothelial ECV304 cells(American Type Culture Collection, Rockville, Md.). Specifically,pC9LPTγ1 or pC2LPTδ were digested with BspH I before electroporatinginto these cell lines with a Cell-Porator™ (Life Technologies,Gaithersburg, Md.). After adherence of the transfected cells 24 hourslater, the cells were grown in the presence of 500 μg/ml Hygromycin B(Hyg) (Calbiochem, La Jolla, Calif.) to select for cells that hadincorporated plasmids. Hyg-resistant clones that expressed LPAAT-γ1 orLPAAT-δ mRNA at a level more than 10 fold higher than that of cellstransfected with pCE9 or pCE2 vector, based on Northern Blot analysis,were selected for further study.

FIG. 13 compares the LPAAT activity in ECV304 cells stably transfectedwith the expression plasmids for LPAAT-α (pCE9.LPAAT-α), LPAAT-β(pCE9.LPAAT-β) DNA, LPAAT-γ1 (pC9LPTγ1), LPAAT-δ (pC2LPTδ), or thecontrol vector (pCE9). This screening assay for LPAAT activity in cellextracts was based on the conversion of [¹⁴C]oleoyl-CoA to [¹⁴C]PA usinga TLC assay. The assay was carried out in total cell extractsresuspended in lysis buffer (Ella, et al., Anal. Biochem. 218: 136–142,1994) supplemented with 50 μM [¹⁴C]oleoyl-CoA and 200 μM LPA. Thesamples were incubated for 10 min, extracted from chloroform, beforeloading onto TLC plates. Lanes 1 and 2 refer to [¹⁴C]oleoyl-CoA and LPAincubated with cell extract transfected with LPAAT-α plasmid; lanes 3and 4, with LPAAT-β plasmid; lanes 5 and 6, with LPAAT-γ1 plasmid; lanes7 and 8, with LPAAT-δ plasmid; and lanes 9 and 10, with control vector.ECV304 cells transfected with LPAAT-α or -β cDNA (lanes 1 to 4) containmore than 3 and 20 times, respectively, LPAAT activity when compared tothose of control cells (lanes 9 and 10) as evidenced by the increasedconversion of [¹⁴C]oleoyl-CoA to [¹⁴C]PA. Cells transfected with LPAAT-δcDNA (lanes 7 and 8) contain about 2.5 times more LPAAT activity thanthose of control cells (lanes 9 and 10), whereas cells transfected withLPAAT-δ cDNA show no increase in activity when compared to those ofcontrol cells (lanes 9 and 10).

1. An isolated polypeptide having lysophosphatidic acid acyltransferaseactivity, comprising the amino acid sequence SEQ ID NO: 15.